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FDA 510(k)

DEKA TAC DEVICE

K-Number: K093915 · 2011-08-23

ApplicantDeka Research & Development Corp.
Decision Date2011-08-23
Product CodeFIG
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

DEKA TAC DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Deka Research & Development Corp.. It received FDA 510(k) clearance on 2011-08-23 under 510(k) number K093915. The device is classified under product code FIG. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DEKA TAC DEVICE?

DEKA TAC DEVICE is a medical device that received FDA 510(k) clearance on 2011-08-23. The listed applicant is Deka Research & Development Corp.. The 510(k) number is K093915.

When did DEKA TAC DEVICE receive FDA 510(k) clearance?

DEKA TAC DEVICE received FDA 510(k) clearance on 2011-08-23, under 510(k) number K093915.

Who is the listed applicant for DEKA TAC DEVICE?

The FDA 510(k) record lists Deka Research & Development Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DEKA TAC DEVICE?

The FDA product code for DEKA TAC DEVICE is FIG.

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Other records listing Deka Research & Development Corp. as applicant

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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